Suv4-20h2 protects against influenza virus infection by suppression of chromatin loop formation

被引:4
|
作者
Shiimori, Masami [1 ]
Ichida, Yu [1 ]
Nukiwa, Ryota [1 ,3 ]
Sakuma, Toshie [1 ]
Abe, Haruka [1 ]
Kajitani, Rei [2 ]
Fujino, Yuji [3 ]
Kikuchi, Akira [4 ]
Kawamura, Takeshi [5 ,6 ]
Kodama, Tatsuhiko [5 ]
Toyooka, Shinichi [7 ]
Shirahige, Katsuhiko [8 ]
Schotta, Gunnar [9 ,10 ]
Kuba, Keiji [11 ]
Itoh, Takehiko [2 ]
Imai, Yumiko [1 ,12 ]
机构
[1] Natl Inst Biomed Innovat Hlth & Nutr NIBIOHN, Lab Regulat Intractable Infect Dis, Osaka 5670085, Japan
[2] Tokyo Inst Technol, Sch & Grad Sch Biosci & Biotechnol, Dept Biol Informat, Tokyo 1528550, Japan
[3] Osaka Univ, Grad Sch Med, Dept Anesthesiol & Intens Care Med, Suita, Osaka 5650871, Japan
[4] Osaka Univ, Grad Sch Med, Dept Mol Biol & Biochem, Osaka 5650871, Japan
[5] Univ Tokyo, Res Ctr Adv Sci & Technol, Lab Syst Biol & Med, Tokyo 1538904, Japan
[6] Univ Tokyo, Isotope Sci Ctr, Prote Lab, Tokyo 1130032, Japan
[7] Okayama Univ, Grad Sch Med, Dept Gen Thorac Surg & Breast & Endocrinol Surg, Okayama 7008558, Japan
[8] Univ Tokyo, Inst Quantitat Biosci, Lab Genome Struct & Funct, Tokyo 1130032, Japan
[9] Ludwig Maximilians Univ Munchen, Biomed Ctr, Dept Mol Biol, D-82152 Munich, Germany
[10] Munich Ctr Integrated Prot Sci CiPS, D-81377 Munich, Germany
[11] Akita Univ, Dept Biochem & Metab Sci, Fac Med, Akita 0108543, Japan
[12] Osaka Univ, Inst Prot Res, Lab Infect Syst, Suita, Osaka 5650871, Japan
关键词
MAMMALIAN GENOMES; COHESIN; CTCF; EXPRESSION; CELLS; HOXC8; IDENTIFICATION; ORGANIZATION; ARCHITECTURE; THERAPY;
D O I
10.1016/j.isci.2021.102660
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The spatial organization of chromatin is known to be highly dynamic in response to environmental stress. However, it remains unknown how chromatin dynamics contributes to ormodulates disease pathogenesis. Here, we showthat upon influenza virus infection, the H4K20me3 methyltransferase Suv4-20h2 binds the viral protein NP, which results in the inactivation of Suv4-20h2 and the dissociation of cohesin from Suv4-20h2. Inactivation of Suv4-20h2 by viral infection or genetic deletion allows the formation of an active chromatin loop at the HoxC8-HoxC6 loci coincident with cohesin loading. HoxC8 and HoxC6 proteins in turn enhance viral replication by inhibiting the Wnt-beta-catenin mediated interferon response. Importantly, loss of Suv4-20h2 augments the pathology of influenza infection in vivo. Thus, Suv4-20h2 acts as a safeguard against influenza virus infection by suppressing cohesin-mediated loop formation.
引用
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页数:26
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